2,793 research outputs found

    Semileptonic decays of BcB_c meson to S-wave charmonium states in the perturbative QCD approach

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    Inspired by the recent measurement of the ratio of BcB_c branching fractions to J/ψπ+J/\psi \pi^+ and J/ψμ+νμJ/\psi \mu^+\nu_{\mu} final states at the LHCb detector, we study the semileptonic decays of BcB_c meson to the S-wave ground and radially excited 2S and 3S charmonium states with the perturbative QCD approach. After evaluating the form factors for the transitions BcP,VB_c\rightarrow P,V, where PP and VV denote pseudoscalar and vector S-wave charmonia, respectively, we calculate the branching ratios for all these semileptonic decays. The theoretical uncertainty of hadronic input parameters are reduced by utilizing the light-cone wave function for BcB_c meson. It is found that the predicted branching ratios range from 10610^{-6} up to 10210^{-2} and could be measured by the future LHCb experiment. Our prediction for the ratio of branching fractions BR(Bc+J/Ψπ+)BR(Bc+J/Ψμ+νμ)\frac{\mathcal {BR}(B_c^+\rightarrow J/\Psi \pi^+)}{\mathcal {BR}(B_c^+\rightarrow J/\Psi \mu^+\nu_{\mu})} is in good agreement with the data. For BcVlνlB_c\rightarrow V l \nu_l decays, the relative contributions of the longitudinal and transverse polarization are discussed in different momentum transfer squared regions. These predictions will be tested on the ongoing and forthcoming experiments.Comment: 12 pages, 3 figures, 5 table

    3-(4-Carb­oxy-5-carboxyl­ato-1H-imidazol-2-yl)pyridin-1-ium monohydrate

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    In the zwitterionic mol­ecule of the title compound, C10H7N3O4·H2O, one carboxyl group is deprotonated and the pyridine N atom is protonated. The pyridinium and imidazole rings form a dihedral angle of 5.23 (1)°. An intramolecular O—H⋯O hydrogen bond occurs. In the crystal, inter­molecular N—H⋯O, O—H⋯N and O—H⋯O hydrogen bonds link the zwitterions and water mol­ecules into sheets parallel to (102)

    2-(2-Hy­droxy-3-meth­oxy­phen­yl)-1H-benzimidazol-3-ium perchlorate

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    In the title mol­ecular salt, C14H13N2O2 +·ClO4 −, the ring systems in the cation are almost coplanar [dihedral angle = 5.53 (13)°]. Intra­molecular N—H⋯O and O—H⋯O hydrogen bonds generate S(6) and S(5) rings, respectively. In the crystal, the two H atoms involved in the intra­molecular hydrogen bonds also participate in inter­molecular links to acceptor O atoms of the perchlorate anions. A simple inter­molecular N—H⋯O bond also occurs. Together, these form a double-chain structure along [101]
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